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The Journal of Investigative Dermatology|November 26, 2010
Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6Eva Riveira-Munoz, Su-Min He, Georgia Escaramís, et al.
The Bone & Joint Journal|May 31, 2024
Cost-effectiveness analysis of soft bandage and immediate discharge versus rigid immobilization in children with distal radius torus fracturesDaniel C Perry, Melina Dritsaki, Juul Achten, et al.
American Journal of Medical Genetics. Part A|September 21, 2016
Phenotype and genotype in 52 patients with Rubinstein-Taybi syndrome caused by EP300 mutationsPatricia Fergelot, Martine Van Belzen, Julien Van Gils, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2026
Nine changes needed to deliver a radical transformation in biodiversity measurementWilliam J Sutherland, Neil D Burgess, Scott V Edwards, et al.
Medrxiv : the Preprint Server for Health Sciences|July 17, 2025
Genome-wide insights into generalised anxiety using a dimensional symptom severity approachMegan Skelton, Brittany L Mitchell, Elham Assary, et al.
Behaviour Research and Therapy|November 13, 2019
The Genetic Links to Anxiety and Depression (GLAD) Study: Online recruitment into the largest recontactable study of depression and anxietyMolly R Davies, Gursharan Kalsi, Chérie Armour, et al.
Nature Human Behaviour|June 9, 2026
Genome-wide meta-analysis of quantitatively measured generalized anxiety symptoms in individuals of European ancestryMegan Skelton, Brittany L Mitchell, Elham Assary, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2023
Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort studyTaila Hartley, Deborah Marshall, Meryl Acker, et al.
Clinical Genetics|November 10, 2022
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing dataTaila Hartley, Élisabeth Soubry, Meryl Acker, et al.
The Lancet. Diabetes & Endocrinology|June 20, 2020
Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort studyStefan Groeneweg, Ferdy S van Geest, Ayhan Abacı, et al.
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